Oxazolidinone Antibacterial Agents. An Enantioselective Synthesis of the [6,5,5] Tricyclic Fused Oxazolidinone Ring System and Application to the Synthesis of a Rigid DuP 721 Analogue-Reference-Cited by-同舟云学术

Oxazolidinone Antibacterial Agents. An Enantioselective Synthesis of the [6,5,5] Tricyclic Fused Oxazolidinone Ring System and Application to the Synthesis of a Rigid DuP 721 Analogue

Published:1996-01-01 Issue:18 Volume:61 Page:6470-6474
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Gleave D. Mark¹,Brickner Steven J.¹

Affiliation:

1. Medicinal Chemistry Research, Pharmacia & Upjohn, Inc., Kalamazoo, Michigan 49001

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo960945s

Reference19 articles.

1. Synthesis and Antibacterial Activity of U-100592 and U-100766, Two Oxazolidinone Antibacterial Agents for the Potential Treatment of Multidrug-Resistant Gram-Positive Bacterial Infections

2. Identification of a Novel Oxazolidinone (U-100480) with Potent Antimycobacterial Activity

3. Regioselective Metalation of Fluoroanilines. An Application to the Synthesis of Fluorinated Oxazolidinone Antibacterial Agents

4. Oxazolidinones, a new class of synthetic antibacterial agents: in vitro and in vivo activities of DuP 105 and DuP 721

5. (b) Wang, C-L. J.; Gregory, W. A.; Wuonola, M. A.Tetrahedron1989,45, 1323.

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